|
|
| ID |
289 |
| OMIM_ID |
154700
|
| Disease |
MARFAN SYNDROME |
| Gene |
FBN1
|
| SNP_ID |
rs5812447
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/T
|
| Orientation |
fwd/T |
| Chr-Number |
15 |
| SNP
type |
N |
| Length |
801 |
| 5'
Near Seq 30 bp |
aagcataatgaagtaaattgtttttttttt |
| 3'
Near Seq 30 bp |
cttctctcttttttacaaagtgttatttta |
| Fasta
Sequence |
CATAATTCAG GTTTGAATCA AGGATTCAAA GCAACCTATG TCCTAAAACA AGGTTTATGA
CTTTGTTTGA AAAAAAGAAA CCATTTTAGA TTTATTAGCA GTTAGTTGAA ACAACAGATT
TTGTGATTTT TGTCAGGTCT TGCCAAATGC ATGTCAAATG TACAAGACCC TCATGTTTAT
GCAGATATTT GTGAGAATGT CTTTAACTGA GATCCAATCC TGTGAATAAA ACCAGTCATG
AATATACATG GAAATTTGCA AAGTCAAGTG TACAGCCCTT TTCTATCTCT CCAACCCTAA
CACTCAGAAT AATATAGATC ATCCTTTCCT AACTCATACG TAATGTCAGG CTCATACTGG
GTTTCAAAAA AAGCATAATG AAGTAAATTG TTTTTTTTTT
N
CTTCTCTCTT TTTTACAAAG TGTTATTTTA AATTGGCAAG GGGTAAATAT CTGTCTTCAG
CTATAAATGT GAAACTAATA TTTCTGCCAG TAATGATCTT CTAACTTTAA AAACAATGTC
CTTAAATCAT TTAATAATTA CATTCCTAAT AATTACATTT CTAATACAGT TCTCTAAGAA
CTACAGTTAA AACCAGAATA AAATATATTC TGTGGACCAA GTTGATGGTA ATTTTAAAAT
CCCTAACATT TATGGGTATA TAACTTTTAA GGATACTAAT GCAGCATCAA CCCAATTGTC
CTTTATTTTG GCTCATCTAA TTTACAGACA TGATTTCTGA AGTTTAACAG TATTTGTAAT
GGCAATATCC AAAGTGATTT TGGCTGAGTA AACTGCTATT
|
|
|
